<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>guosheng Wang</submitter><organism>Rattus norvegicus</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16153</full_dataset_link><description>We constructed a rat model of femoral osteomyelitis by injecting a mixture of Staphylococcus aureus suspension and LPS.  Subsequently, we performed RNA-seq to compare the osteomyelitic femur with the normal femur group.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - In this study, five femoral tissue samples were collected from the chronic osteomyelitis model group and the control group each, resulting in a total of ten samples.</sample_protocol><sample_protocol>Library Construction - For each sample, 500 ng of total RNA was used for cDNA synthesis via a strand-switching reverse transcription approach. The resulting cDNA was then amplified by PCR, followed by barcoding with the Native Barcode kit (SQK-NBD114.96) and purification using Ampure XP Beads. Finally, 300 fmol of the resulting library was loaded onto a PromethION flow cell (vR10.4.4) for sequencing.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA extraction using Total RNA extraction Kit (DP431, TIANGEN, China). The quality and quantity of the purified RNA were determined by measuring the absorbance at 260nm/280nm(A260/A280) using Ultrafine spectrophotometer (N50 touch, IMPLEN, Germany). The integrity of RNA was further verified by 1.0% agarose gel electrophoresis</sample_protocol><sample_protocol>Sequencing - We used the Oxford nanopore technology (ONT) to sequence from AS and HC</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Data Transformation - To evaluate the accuracy of abundance estimation with transcript and gene resolution, we used the quasi-mapping mode of Salmon(v1.7.0) [17] to estimate the TPM for each transcript and gene in each of the sample data.</data_protocol><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>PromethION</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Rattus norvegicus</species><pubmed_authors>guosheng Wang</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-seq of rat tissues with chronic osteomyelitis</name><description>We constructed a rat model of femoral osteomyelitis by injecting a mixture of Staphylococcus aureus suspension and LPS.  Subsequently, we performed RNA-seq to compare the osteomyelitic femur with the normal femur group.</description><dates><release>2025-12-10T00:00:00Z</release><modification>2026-05-30T17:25:19.459Z</modification><creation>2025-11-11T14:59:52.041Z</creation></dates><accession>E-MTAB-16153</accession><cross_references><ENA>ERP184213</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>